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SPIB (Spi-B transcription factor)

Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
6689
Gene nameGene Name - the full gene name approved by the HGNC.
Spi-B transcription factor
Gene symbolGene Symbol - the official gene symbol approved by the HGNC, which is a short abbreviated form of the gene name.
SPIB
SynonymsGene synonyms aliases
SPI-B
ChromosomeChromosome number
19
Chromosome locationChromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
19q13.33
SummarySummary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a transcriptional activator that binds to the PU-box (5`-GAGGAA-3`) and acts as a lymphoid-specific enhancer. Four transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep
miRNAmiRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT661108 hsa-miR-3664-5p HITS-CLIP 23824327
MIRT661107 hsa-miR-6504-3p HITS-CLIP 23824327
MIRT661106 hsa-miR-4639-3p HITS-CLIP 23824327
MIRT661105 hsa-miR-5693 HITS-CLIP 23824327
MIRT661104 hsa-miR-6499-3p HITS-CLIP 23824327
Transcription factors
Transcription factor Regulation Reference
POU2AF1 Unknown 24801987
POU2F2 Unknown 24801987
Gene ontology (GO)Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000785 Component Chromatin ISA
GO:0000978 Function RNA polymerase II cis-regulatory region sequence-specific DNA binding IMP 10196196
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA 21873635
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific ISA
GO:0001228 Function DNA-binding transcription activator activity, RNA polymerase II-specific IMP 10196196
Other IDsOther ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM
HGNC
e!Ensembl
Protein
UniProt ID Q01892
Protein name Transcription factor Spi-B
Protein function Sequence specific transcriptional activator which binds to the PU-box, a purine-rich DNA sequence (5'-GAGGAA-3') that can act as a lymphoid-specific enhancer. Promotes development of plasmacytoid dendritic cells (pDCs), also known as type 2 DC p
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00178 Ets
170 252
Ets-domain
Domain
Sequence
MLALEAAQLDGPHFSCLYPDGVFYDLDSCKHSSYPDSEGAPDSLWDWTVAPPVPATPYEA
FDPAAAAFSHPQAAQLCYEPPTYSPAGNLELAPSLEAPGPGLPAYPTENFASQTLVPPAY
APYPSPVLSEEEDLPLDSPALEVSDSESDEALVAGPEGKGSEAGTRKKLRLYQFLLGLLT
RGDMRECVWWVEPGAGVFQFSSKHKELLARRWGQQKGNRKRMTYQKLARALRNYAKTGEI
RKVKRKLTYQFD
SALLPAVRRA
Sequence length 262
Interactions View interactions
Associated diseases
Causal
Disease name Disease term dbSNP ID References
Liver failure Liver Failure rs118203990, rs118203991, rs118203992, rs387907022, rs201861847, rs796065037, rs759315662, rs368196005, rs796052121, rs369437593, rs367683258, rs766314948, rs368085185, rs770446752, rs753039116, rs776797592, rs1490906786, rs1562849964, rs759960319, rs776597537, rs375350359, rs1573008071, rs1601977105, rs1174791046, rs1019313682
Osteoporosis Osteoporosis rs72658152, rs72667023, rs587776916, rs72656370, rs768615287
Unknown
Disease name Disease term dbSNP ID References
Biliary cholangitis Primary biliary cholangitis, Secondary Biliary Cholangitis 20639880
Biliary cirrhosis Biliary cirrhosis, Biliary Cirrhosis, Primary, 1, Primary biliary cirrhosis 20639880, 21399635, 20639880, 21399635, 20639880, 26394269
Celiac disease Celiac Disease rs2305764, rs35218876
Cirrhosis Cirrhosis rs119465999, rs144369314, rs8056684, rs112053857, rs75998507

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